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MYC (p.T73P)

Variant Data

Location

  • HGVS: ENST00000377970:c.217A>C
  • Reference Version: GRCh37
  • Chromosome: 8
  • Start: 128750680
  • Stop: 128750680
  • Strand: 1
  • Transcript: ENST00000377970 (ensembl - 74_37)
  • Gene: MYC ( View drug interactions on DGIdb )

Information

  • Reference: A
  • Variant: C
  • Amino Acid: p.T73P
  • Mutation Type: missense
  • Variant Type: SNV (SO:0001483)
  • cDNA Change: c.217
  • Tags: likely pathogenic

Disease Data

Disease Source Batch Tags External Links
skin melanoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
neuroblastoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
non-Hodgkin lymphoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
lung adenocarcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
esophageal carcinoma Chang et al., 2016, Nat. Biotechnol. Pan-cancer recurrent hotspots (View variants) likely pathogenic
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